pCMV-N2-6MYC-hMID2
(Plasmid
#51035)
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Purposemammalian expression of myc-tagged human MID2
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 51035 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCMV-N2-6Myc
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Backbone manufacturerCox lab
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Modifications to backboneVector is modified from the pEGFP-N2 vector (Clontech, Palo Alto, CA). Briefly, the GFP coding region was excised from pEGFP-N2 with NotI and BamHI, the 5' overhangs filled using T4 DNA polymerase and the vector religated to give pCMV-N2. Six copies of the myc epitope containing a start codon was amplified from pGEM-6mycT (gift from M. Whitelaw, University of Adelaide), and cloned into the HindIII site of pCMV-N2.
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Vector typeMammalian Expression
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Selectable markersNeomycin (select with G418)
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberUnknown
Gene/Insert
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Gene/Insert nameMID2
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SpeciesH. sapiens (human)
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Entrez GeneMID2 (a.k.a. FXY2, MRX101, RNF60, TRIM1)
- Promoter CMV
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Tag
/ Fusion Protein
- MYC (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI (not destroyed)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer CMV-F
- 3′ sequencing primer SV40pA-R (Common Sequencing Primers)
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
Please note: hMID2 begins at residue 19 of the NCBI reference sequence.
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.
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For your Materials & Methods section:
pCMV-N2-6MYC-hMID2 was a gift from Timothy Cox (Addgene plasmid # 51035 ; http://n2t.net/addgene:51035 ; RRID:Addgene_51035) -
For your References section:
MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders. Short KM, Hopwood B, Yi Z, Cox TC. BMC Cell Biol. 2002;3:1. Epub 2002 Jan 4. 10.1186/1471-2121-3-1 PubMed 11806752